TY - JOUR
T1 - Proposal for a Novel Classification of Patients With Enlarged Ventricles and Cognitive Impairment Based on Data-Driven Analysis of Neuroimaging Results in Patients With Psychiatric Disorders
AU - Yasuda, Yuka
AU - Ito, Satsuki
AU - Matsumoto, Junya
AU - Okada, Naohiro
AU - Onitsuka, Toshiaki
AU - Ikeda, Masashi
AU - Kushima, Itaru
AU - Sumiyoshi, Chika
AU - Fukunaga, Masaki
AU - Nemoto, Kiyotaka
AU - Miura, Kenichiro
AU - Hashimoto, Naoki
AU - Ohi, Kazutaka
AU - Takahashi, Tsutomu
AU - Sasabayashi, Daiki
AU - Koeda, Michihiko
AU - Yamamori, Hidenaga
AU - Fujimoto, Michiko
AU - Takano, Harumasa
AU - Hasegawa, Naomi
AU - Narita, Hisashi
AU - Yamamoto, Maeri
AU - Tha, Khin Khin
AU - Kikuchi, Masataka
AU - Kamishikiryo, Toshiharu
AU - Itai, Eri
AU - Okubo, Yoshiro
AU - Tateno, Amane
AU - Nakamura, Motoaki
AU - Kubota, Manabu
AU - Igarashi, Hiroyuki
AU - Hirano, Yoji
AU - Okada, Go
AU - Miyata, Jun
AU - Numata, Shusuke
AU - Abe, Osamu
AU - Yoshimura, Reiji
AU - Nakagawa, Shin
AU - Yamasue, Hidenori
AU - Ozaki, Norio
AU - Kasai, Kiyoto
AU - Hashimoto, Ryota
N1 - Publisher Copyright:
© 2025 The Author(s). Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology.
PY - 2025/3
Y1 - 2025/3
N2 - One of the challenges in diagnosing psychiatric disorders is that the results of biological and neuroscience research are not reflected in the diagnostic criteria. Thus, data-driven analyses incorporating biological and cross-disease perspectives, regardless of the diagnostic category, have recently been proposed. A data-driven clustering study based on subcortical volumes in 5604 subjects classified into four brain biotypes associated with cognitive/social functioning. Among the four brain biotypes identified in controls and patients with schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorder, and other psychiatric disorders, we further analyzed the brain biotype 1 subjects, those with an extremely small limbic region, for clinical utility. We found that the representative feature of brain biotype 1 is enlarged lateral ventricles. An enlarged ventricle, defined by an average z-score of left and right lateral ventricle volumes > 3, had a sensitivity of 99.1% and a specificity of 98.1% for discriminating brain biotype 1. However, the presence of an enlarged ventricle was not sufficient to classify patient subgroups, as 1% of the controls also had enlarged ventricles. Reclassification of patients with enlarged ventricles according to cognitive impairment resulted in a stratified subgroup that included patients with a high proportion of schizophrenia diagnoses, electroencephalography abnormalities, and rare pathological genetic copy number variations. Data-driven clustering analysis of neuroimaging data revealed subgroups with enlarged ventricles and cognitive impairment. This subgroup could be a new diagnostic candidate for psychiatric disorders. This concept and strategy may be useful for identifying biologically defined psychiatric disorders in the future.
AB - One of the challenges in diagnosing psychiatric disorders is that the results of biological and neuroscience research are not reflected in the diagnostic criteria. Thus, data-driven analyses incorporating biological and cross-disease perspectives, regardless of the diagnostic category, have recently been proposed. A data-driven clustering study based on subcortical volumes in 5604 subjects classified into four brain biotypes associated with cognitive/social functioning. Among the four brain biotypes identified in controls and patients with schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorder, and other psychiatric disorders, we further analyzed the brain biotype 1 subjects, those with an extremely small limbic region, for clinical utility. We found that the representative feature of brain biotype 1 is enlarged lateral ventricles. An enlarged ventricle, defined by an average z-score of left and right lateral ventricle volumes > 3, had a sensitivity of 99.1% and a specificity of 98.1% for discriminating brain biotype 1. However, the presence of an enlarged ventricle was not sufficient to classify patient subgroups, as 1% of the controls also had enlarged ventricles. Reclassification of patients with enlarged ventricles according to cognitive impairment resulted in a stratified subgroup that included patients with a high proportion of schizophrenia diagnoses, electroencephalography abnormalities, and rare pathological genetic copy number variations. Data-driven clustering analysis of neuroimaging data revealed subgroups with enlarged ventricles and cognitive impairment. This subgroup could be a new diagnostic candidate for psychiatric disorders. This concept and strategy may be useful for identifying biologically defined psychiatric disorders in the future.
KW - cognitive impairment
KW - copy number variation
KW - data-driven analysis
KW - enlarged ventricles
KW - schizophrenia
UR - http://www.scopus.com/inward/record.url?scp=85219528250&partnerID=8YFLogxK
U2 - 10.1002/npr2.70010
DO - 10.1002/npr2.70010
M3 - 学術論文
C2 - 40011069
AN - SCOPUS:85219528250
SN - 2574-173X
VL - 45
JO - Neuropsychopharmacology Reports
JF - Neuropsychopharmacology Reports
IS - 1
M1 - e70010
ER -